Global Development Lead, Internal Medicine (MD, Sr. Director) (Internal Medicine)

Location: United States — New York — New York City. Hybrid role requiring residence within commuting distance and on-site work an average of 2.5 days per week. Up to 30% travel may be required.

Annual base salary: $274,500–$457,500. The role also includes a 25% bonus target and eligibility for a share-based long-term incentive program.

Company

hirify.global is a biopharmaceutical company developing medicines and conducting global clinical research.

What you will do

• Lead the cross-functional Clinical Development Team for assigned Internal Medicine assets across clinical, pharmacology, statistics, safety, commercial, patient access, and operations.
• Create and secure endorsement for comprehensive Clinical Development Plans, pediatric investigation plans, and study protocol design documents.
• Design, execute, interpret, and report late-stage clinical trials supporting worldwide regulatory submissions and reimbursement.
• Provide medical and therapeutic-area expertise for clinical data review, adverse-event interpretation, safety monitoring, statistical analysis plans, and database releases.
• Lead submission-level deliverables, including SCE, SCS, IAP, IARP, TLFs, DSURs, PBRERs, safety narratives, and product-label materials.
• Engage regulators, steering committees, data monitoring and adjudication committees, patient advocates, and other external stakeholders to shape development strategy.

Requirements

• MD or DO degree.
• Endocrinology or internal medicine background with cardiometabolic late-stage development experience, including type 2 diabetes.
• 8+ years of relevant experience and a successful track record in academic and/or biopharmaceutical clinical research and development.
• Extensive knowledge of clinical development, global and regional regulations, ICH/GCP, and adverse-event management.
• Demonstrated medical, scientific, administrative, project-management, communication, and large-team leadership capabilities.
• Permanent U.S. work authorization is required; U.S. work visa sponsorship is not available now or in the future.

Nice to have

• Experience designing and launching large clinical development teams.
• Experience providing specialized medical monitoring support.
• Experience with digital innovation and patient engagement strategies.

Culture & Benefits

• Work in a complex, cross-functional matrix environment with responsibility for influencing and aligning clinical development teams.
• Benefits include a 401(k) plan with company matching and an additional retirement savings contribution.
• Paid vacation, holidays, personal days, caregiver and parental leave, and medical leave.
• Medical, prescription drug, dental, and vision coverage.
• Relocation assistance may be available based on business needs and eligibility.